HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782343del , CM000663.2:g.58782343del | GRCh38 |
NC_000001.10:g.59248015del , CM000663.1:g.59248015del | GRCh37 |
NC_000001.9:g.59020603del | NCBI36 |
NG_047027.1:g.6775del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.798del | ENSP00000518166.1:p.Ile267SerfsTer16 | |
ENST00000371222.4:c.732del MANE Select | ENSP00000360266.2:p.Ile245SerfsTer16 | |
ENST00000678696.1:c.732del | ENSP00000503132.1:p.Ile245SerfsTer16 | |
ENST00000371222.3:c.732del | ENSP00000360266.2:p.Ile245SerfsTer16 | |
NM_002228.3:c.732del | NP_002219.1:p.Ile245SerfsTer16 | |
NM_002228.4:c.732del MANE Select | NP_002219.1:p.Ile245SerfsTer16 |